BSG basigin (Ok blood group)

Information
Symbol
BSG
Type
protein-coding
Description
basigin (Ok blood group)
Entrez Gene ID
682
Genome
hg19
Position
chr19:572,596-583,493
Genome
hg38
Position
chr19:572,596-583,493
MIM
109480 OMIM
HGNC
HGNC:1116 HGNC
Ensembl
ENSG00000172270 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 18
Likely benign 0 12
Affects 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
56
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
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Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM 5F7
SYNONYM CD147
SYNONYM EMMPRIN
SYNONYM EMPRIN
SYNONYM HAb18G
SYNONYM OK
SYNONYM TCSF
MIM 109480 OMIM
HGNC HGNC:1116 HGNC
Ensembl ENSG00000172270 Ensembl
AllianceGenome HGNC:1116
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000680326.1 hg38 chr19 572,610 583,493 10,884
ENST00000618006.4 hg38 chr19 572,619 583,487 10,869
ENST00000614867.2 hg38 chr19 572,623 583,487 10,865
ENST00000680552.1 hg38 chr19 572,529 583,442 10,914
ENST00000576984.3 hg38 chr19 575,213 583,493 8,281
ENST00000545507.6 hg38 chr19 571,277 583,493 12,217
ENST00000346916.9 hg38 chr19 571,310 583,493 12,184
ENST00000353555.9 hg38 chr19 572,596 583,493 10,898
ENST00000573784.6 hg38 chr19 575,047 583,494 8,448
ENST00000679472.1 hg38 chr19 572,529 583,442 10,914
ENST00000680065.1 hg38 chr19 572,529 583,462 10,934
ENST00000333511.9 hg38 chr19 572,596 583,493 10,898
ENST00000346916.9 hg19 chr19 571,310 583,493 12,184
ENST00000333511.9 hg19 chr19 572,596 583,493 10,898
ENST00000545507.6 hg19 chr19 571,277 583,493 12,217
ENST00000353555.9 hg19 chr19 572,596 583,493 10,898
ENST00000573784.6 hg19 chr19 575,047 583,494 8,448
ENST00000576984.3 hg19 chr19 575,213 583,493 8,281
ENST00000614867.2 hg19 chr19 572,623 583,487 10,865
ENST00000618006.4 hg19 chr19 572,619 583,487 10,869
ENST00000679472.1 hg19 chr19 572,529 583,442 10,914
ENST00000680065.1 hg19 chr19 572,529 583,462 10,934
ENST00000680326.1 hg19 chr19 572,610 583,493 10,884
ENST00000680552.1 hg19 chr19 572,529 583,442 10,914
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